Effect of sulfur and composted manure on SO4-S,P and micronutrient availability in a calcareous saline–sodic soil

A factorial design with different levels of elemental S and cow manure was used to investigate the effects of S and manure on SO₄-S, P and micronutrient availability in a calcareous saline–sodic soil. The results revealed that the recovery of SO₄-S increased significantly (p≤0.05) in all treatments as elemental S increased, particularly when in combination with manure. The interactional effects of S° and manure application rates resulted in a decrease in soil pH of 0.1 to 0.9 units and increases in soil EC from 0.1 to 2.6 dS m^?1 as result of an increase in the number of oxidisers and the oxidation rate of elemental S. Application of S° in combination with manure led to an increase in soil-available-P (0.6–40 mg kg^?1), DTPA-Zn (0.2–3.9 mg kg^?1) and DTPA-Fe (0.1–5.6 mg kg^?1).     

腐殖酸对As(V)在覆铁砂介质中吸附行为的影响

对腐殖酸(HA)进行了成分分析及红外表征,并从HA浓度、pH值、As(Ⅴ)初始浓度等方面,研究了HA对As(Ⅴ)在覆铁砂介质中吸附行为的影响.结果表明,随着HA浓度的升高,总砷去除率逐渐降低.当HA浓度增加到25mg.l-1时,与不存在HA条件下相比,总砷去除率降低了12%左右.溶液pH值影响As(Ⅴ)的去除,pH值从6升高到8时,总砷去除率从52.1%降到了39%.其中的作用机理主要是HA与As(Ⅴ)在覆铁砂表面形成竞争吸附,HA争夺了As(Ⅴ)的吸附点位.此外,HA与Fe(Ⅲ)的络合作用也是导致覆铁砂对砷的去除率降低的一个重要原因.     

滤速对慢滤池深度处理生活污水的影响

为进一步提高再生水水质,将慢滤池用于污水二级处理出水的进一步处理。选取浊度、COD、色度和细菌总数4个指标,利用实验室小试装置,研究了0.1、0.3、0.5m/h这3种滤速下慢滤池的性能。结果表明,滤速由0.1m/h升高至0.3m/h时,慢滤池出水水质略有下降。而滤速由0.3m/h升高至0.5m/h时,慢滤池出水水质下降显著。滤速小于等于0.3m/h时,慢滤出水浊度、COD、色度和细菌总数平均为0.4NTU、25.9mg/L、14.9°、5×10^3CFU/mL。慢滤对这4个指标的平均去除率分别为78.6%、36.0%、34.0%、62.3%。为获得优良的水质,建议慢滤池用于污水深度处理时,滤速宜小于0.3m/h。但实际工程中,用户对再生水水质要求不高时,则可适当增大慢滤池滤速。     

有机酸-铁改性活性炭去除饮用水中的砷

利用有机酸(柠檬酸和EDTA)螯合铁加载来改性活性炭,采用动态活性炭小柱进行吸附穿透实验来检测改性后活性炭对砷的吸附能力.研究表明,加载到活性炭上的铁的量随着有机酸和铁浓度增加而增加,在EDTA和铁的浓度分别为0.1mol/L时,活性炭上的铁含量从未加载时的0.24%升至6.18%.改性后的活性炭对砷吸附能力有显著增加,EDTA-Fe改性后的活性炭对As(V)和As(III)穿透时,运行的床体积达到未改性活性炭的10倍.一般情况下,低pH对As(V)的吸附有利.在水体常见pH值范围内(pH 6~9),As(III)的吸附受到影响较小.活性炭上用有机酸螯合法加载的铁大部分以不定形的形式存在,且晶体化效果不明显.     

钢渣中磁性矿物的赋存特性对分选效果的影响研究

对新余钢铁公司0～10 mm的细粒钢渣干式磁选分离所得到的产品进行扫描电镜检测、分析,找出了影响细粒钢渣干式磁选指标难以得到提高的原因,用于指导生产实践。研究结果表明:钢渣在干式磁选过程中,包裹有微细粒的金属铁或与金属铁连生的浮氏体以及具有一定磁性的铁酸盐容易进入磁性分离物中,这些物质自身铁品位较低,从而造成了磁性分离物中铁品位的降低。     

Phytoaccumulation of iron by callus tissue of Clerodendrum indicum (L)

Clerodendrum indicum (L.) is one of the important medicinal plants, originating in India. The plant is used as medicine for bronchitis, asthma and different immunological disease. Micro-propagation is a quick method, producing a huge number of plants. Apical leaf of Clerodendrum indicum (L.) was used as an explant for callogenesis. The combinations of different plant growth regulators (2,4-D, NAA, KN) in MS (Murashige and Skoog) medium produced two types of calli: one was friable and loose and the other was green, embryogenic and compact. Heavy metals cause pollution and health hazards. The plant absorbs heavy metals, which is very useful for controlling environmental pollution. Iron is a major nutrient for both plants and animals, but hyper accumulation of iron is injurious to health. Calli were used to study the optimum conditions of iron uptake in presence of different chemical environments. The different environments were created by using different chemical reagents such as (HCL, HNO₃, H₃PO₄ and KNO₃). Iron (III) was spiked with radioactive Fe-59 and dynamics of uptake was followed by measuring radioactivity by gamma-ray spectrometer. The best condition of iron uptake corresponded to 1 mol L^?1 KNO₃ after 4 hour of equilibration.     

Acid mine drainage attenuation by inhibition of pyrite bioleaching using limestone and olive pomace

The control and inhibition of pyrite bioleaching involved in the generation of acid mine drainage was studied. Inhibition of pyrite bioleaching was performed by varying the pyrite concentration in the medium (substrate inhibition) and/or by addition of limestone (inhibition by pH increase) and olive pomace (inhibition by organic compounds). Inhibition tests of pyrite bioleaching were performed according to a full factorial design with three factors (pyrite, limestone and olive pomace) taken at two levels. Preliminary pyrite bioleaching tests showed the ability of the available inoculum to oxidise the mineral. Subsequently, experimental data for total soluble iron denoted strong inhibition under all the different operating conditions of the factorial design, except when larger pyrite concentrations were used. In particular, inhibition by limestone was due to the increase in pH which negatively affects microorganisms, while inhibition by olive pomace may be related to the antioxidant properties of polyphenols. Interactions among operating conditions were specifically assessed by analysis of variance. Only limestone and/or pomace addition resulted in a significant (95%) diminution of iron extraction.     

Color removal efficiency of dyes using nanozerovalent iron treatment

In this study, zerovalent iron nanoparticles (Fe⁰) were synthesized by chemical reduction method using ferric chloride hexahydrate (FeCl₃?·?6H₂O) as a starting material. Sodium borohydride (NaBH₄) was used as a reducer. The synthesized nanozerovalent iron (NZVI) was separated using magnets. The X-ray diffraction pattern of iron (Fe) nanoparticles showed that the presence of intensive diffraction peak at 2θ value of 45.33° from the lattice plane of face-centered cubic Fe unequivocally indicates that the particles are made of pure Fe. The size of the synthesized NZVI was found to be 16.64?nm. The scanning electron micrograph revealed that the particles have a hexagonal and spherical shape in nature. EDX showed the surface atomic distribution and chemical composition of NZVI. The decolorization efficiency rose with increasing concentration of nanoparticles as well as with time. Maximal color removal efficiency was 90.72% when using 0.5?g/100?mL Fe nanoparticle for acridine orange. Data revealed that the function of NZVI on color removal efficiency was statistically significant. The correlation coefficient between NZVI concentration and time showed a strong negative correlation for dyes used in the experiment.     

Speciation studies on simulated gastro‐intestinal digests of foodstuffs†

The factors affecting the solubilisation of metals during digestion of food have been examined in a two‐stage model system comprising simulated gastric and intestinal juices. The solubilisation of iron, copper and zinc was examined in digests of white and wholemeal bread. Zinc solubility was principally governed by pH and the simulated digestion had little additional effect. In contrast both iron and copper solubility were markedly affected by digestion of the bread. In the case of copper the enzymolysis increased solubility appreciably at neutral pH. All of the cadmium in a simulated gastric digest of canned crab meat was associated with soluble low molecular weight species of less than 1000 daltons. Cadmium solubility resulted from the acidic conditions of the digest rather than enzymatic solubilisation of binding proteins. Ninety percent of the cadmium in the digest became rebound to the insoluble fraction on adjustment to pH7.0. Subsequent simulated intestinal digestion increased the level of soluble cadmium to 20%; 1.0–1.5% was associated with soluble species in the range 26,000–37,000 daltons and 15.0–20.0% with soluble species of less than 3,000 daltons.     

零价铁还原和过硫酸盐氧化联合降解水中硝基苯

将零价铁(Fe0)的还原和过硫酸盐(persulfate,PS)的高级氧化技术结合用于水中难降解有机污染物硝基苯的去除.研究结果表明,Fe0在常温常压下可将硝基苯还原生成苯胺,随着Fe0投加量的增加,硝基苯还原为苯胺的速率逐渐增大.PS本身对硝基苯氧化作用不明显,但在Fe0与PS二者联合体系中,硝基苯和苯胺同时被去除,而且随着PS投加量的增加二者被去除的速度也随之增加.在Fe0还原和PS氧化联合处理硝基苯的体系中可能存在两个过程,一是Fe0还原硝基苯产生苯胺和二价铁离子Fe2+,二是Fe2+催化PS产生强氧化性的硫酸根自由基将苯胺氧化降解.